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The CMA has accepted commitments offered by Google that address the CMA’s competition concerns resulting from investigating Google’s proposals to remove third-party cookies and other functionalities from its Chrome browser.
Payments on account in civil cases, inquests, police station remote attendance, mental health tribunals, family hearings, and travel and mileage.
Events courses and programmes to develop skills, knowledge and networks for chief executive officers, deputy-CEOs and their equivalents in public service.
Urgent safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
This factsheet outlines the domestic control measures that apply to cannabis, cannabidiol (CBD) and controlled cannabinoids.
How to use a case-control study to evaluate your digital health product.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Working with contract management and accreditation.
Interim guidance and information on the law for healthcare professionals
Find out about the symptoms of COVID-19, what to do if you or your child has them and when to get medical help.
Check the tariff classification for antimicrobial bathing systems.
Report from the Advisory Council on the Misuse of Drugs (ACMD) on consumer cannabidiol (CBD) products.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Order a certificate of free sale to export medical devices outside the UK.
How test manufacturers or distributors can apply for approval of their tests to sell on the UK market.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Guidance for industry on flexible approaches we are taking on good distribution practices.
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